Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004468406

FEI Number

3004468406

Entity Name

CHINOOK MEDICAL GEAR, INC.

City/State/Country

Tulsa, OK, US

Establishment Address

12505 E 55th Street, Unit B, Tulsa, OK 74146, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Altitude Technologies, Inc DBA Chinook Medical Gear (Owner Number: 10030316)

Owner / Operator Contact Address

12505 E. 55th St., Unit B, Tulsa, OK 74146, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Pressure Injury Prevention Kit FS EZ IO Kit Manual 6PK

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
POQ	Blood Transfusion Kit	General Hospital	Class 2	880.5440	2016-07-25
OHR	Catheter Care Tray	Gastroenterology, Urology	Class 2	876.5130	2015-02-02
OVN	Suture Kit	General, Plastic Surgery	Class 2	878.4830	2015-03-27
LRR	First Aid Kit With Drug	Unknown	Class N	N/A	2015-03-30
KYZ	Syringe, Irrigating (Non Dental)	General Hospital	Class 1	880.6960	2015-03-27
OGW	Tracheostomy Kit	Anesthesiology	Class 2	868.5800	2014-03-21
GBX	Catheter, Irrigation	General, Plastic Surgery	Class 1	878.4200	2013-11-15
LRS	I.V. Start Kit	General Hospital	Class 2	880.5200	2020-02-28
OFX	General Purpose Dental Tray	Dental	Class 1	872.6640	2014-10-06
KME	Bedding, Disposable, Medical	General Hospital	Class 1	880.6060	2015-03-30
ILI	Sling, Arm	Physical Medicine	Class 1	890.3640	2014-11-26
OHO	First Aid Kit Without Drug	General, Plastic Surgery	Class 1	878.4014	2015-03-27
CAE	Airway, Oropharyngeal, Anesthesiology	Anesthesiology	Class 1	868.5110	2015-03-30
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2024-02-14
GAA	Needle, Aspiration And Injection, Disposable	General, Plastic Surgery	Class 1	878.4800	2015-03-30
OEV	Cardiopulmonary Resuscitation Aid Kit	Anesthesiology	Class 2	868.5915	2021-01-13

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Altitude Technologies, Inc DBA Chinook Medical Gear

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K812404	Nu Tech Medical Systems	BUTTERFLY NEEDLE ASSEMBLY	1981-09-09
K781371	Ferris Mfg. Corp.	BONE MARROW ASPIRATION KIT	1978-09-20

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2014	King Systems Corp.	1	King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.
Z-0002-2022	Bard Peripheral Vascular Inc	2	REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796
Z-0017-2023	Hobbs Medical, Inc.	1	Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620
Z-0018-2023	Hobbs Medical, Inc.	1	Hobbs Transbronchial Aspiration Needle Catalog Number: 4621
Z-0023-2011	Becton Dickinson & Company	1	BD 30G1/2 PrecisionGlide Needle;Catalog/Lot Number: 305106. Needles are intended for use in aspiration and injection of medications.

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3034669683	HUZHOU JUNDA INDUSTRY CO., LTD.	Anji Zhejiang, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004468406. Last updated year: 2026. Please use registration number 3004468406 when referencing this establishment in official correspondence.